Berger R, Le Coniat M, Gendron M C
INSERM U 301, Institut de Génétique Moléculaire, Paris, France.
Cancer Genet Cytogenet. 1993 Aug;69(1):13-6. doi: 10.1016/0165-4608(93)90104-t.
The experience with cytogenetic and flow cytometry methods used for the diagnosis of Fanconi anemia (FA) in one center is summarized. The tests consist of chromosomal breakage and cell cycle studied after sensitization by the introduction of nitrogen mustard into phytohemagglutinin-stimulated blood-cell cultures. The cytogenetic test was shown to be reliable in ascertaining the diagnosis of FA. Flow cytometry studies showed a marked increase in the percentage of cells in G2/M phase in FA patients after sensitization by nitrogen mustard. This increase, however, could not be detected in three FA patients with myelodysplasia or acute leukemia and the results were ambiguous on three occasions.
本文总结了某一中心使用细胞遗传学和流式细胞术方法诊断范可尼贫血(FA)的经验。检测包括染色体断裂以及在将氮芥引入植物血凝素刺激的血细胞培养物致敏后研究细胞周期。结果表明,细胞遗传学检测在确定FA诊断方面是可靠的。流式细胞术研究显示,氮芥致敏后FA患者G2/M期细胞百分比显著增加。然而,在3例患有骨髓发育异常或急性白血病的FA患者中未检测到这种增加,且有3次结果不明确。